US2834771A - Gelatin derivatives and their preparation - Google Patents
Gelatin derivatives and their preparation Download PDFInfo
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- US2834771A US2834771A US556796A US55679656A US2834771A US 2834771 A US2834771 A US 2834771A US 556796 A US556796 A US 556796A US 55679656 A US55679656 A US 55679656A US 2834771 A US2834771 A US 2834771A
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- gelatin
- solution
- derivative
- carbon dioxide
- calcium hydroxide
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- A—HUMAN NECESSITIES
- A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
- A23J—PROTEIN COMPOSITIONS FOR FOODSTUFFS; WORKING-UP PROTEINS FOR FOODSTUFFS; PHOSPHATIDE COMPOSITIONS FOR FOODSTUFFS
- A23J3/00—Working-up of proteins for foodstuffs
- A23J3/04—Animal proteins
- A23J3/06—Gelatine
Definitions
- This invention relates to the production of a gelatin derivative.
- the derivative produced involves the reaction of carbon dioxide and calcium ions with carboxy and amino groups in the gelatin molecule.
- the gelatin derivative will be referred to as carbamino gelatin.
- This gelatin derivative has shown improvements in viscosity and bloom over the unmodified gelatin.
- As a whipping agent it produces a larger overrun in a shorter period of Whipping time than unmodified gelatin samples.
- a stable foam is formed which holds its volume and texture.
- the carbamino gelatin can be used as a whipping agent in the production of any of the edible or inedible foams in which gelatin, or gelatin plus other whipping adjuncts such as hydrolyzed soy protein are employed.
- whipping compositions in which this gelatin derivative can be used successfully are marshmallow preparations, coon desserts, icings, and sugar whips generally.
- EXAMPLE 1 Calcium hydroxide is dispersed in an aqueous solution of neutral 250 bloom gelatin to raise the pH of the solution to about 9. An excess of carbon dioxide gas is then bubbled into the reaction mixture until the mixture is brought down to about pH 7. As the carbon dioxide is bubbled into the reaction mixture, the gelatin derivative of the present invention is formed and calcium carbonate is precipitated. Excess calcium salts (calcium carbonate and calcium hydroxide) are removed by suitable ion exchange resins. The solution containing the derivative is allowed to gel, and then is tunnel dried and ground. The product is more easily dispersed than the unmodified gelatin starting material and is soluble in water at 65 C.
- Carbamino gelatin substantially soluble in cold water, is prepared according to the following method: 88.9 lbs. of water are weighed out into a jacketed kettle. 11.1 lbs. of 250 bloom gelatin are added to the cold water with agitation, and the gelatin dispersion is heated to 2,834,771 Patented May 13, 1958 40-45 C. to dissolve the gelatin. Calcium hydroxide is added to the hot gelatin solution until the pH is raised to between 9.5 and 10.0. Carbon dioxide is then bubbled through the gelatin solution for 15 minutes while the pH of the solution is maintained between 9.5 and 10.0 by the addition of calcium hydroxide.
- the reaction mixture is filtered to remove undissolved lime and calcium carbonate and is placed back into the jacketed kettle with Rohm and Haas IR45 and IR mixed ion exchange resin to remove extraneous anions and cations.
- the solution is filtered again to remove the ion exchange material.
- Theproduct solution is then dried in the sol state by drying on a double drum drier, although any method of drying the gelatin derivatives whereby the sol state is preserved during dehydration is acceptable.
- the dried product is ground in a Fitzpatrick mill.
- the dried prodnot is soluble in relatively cold water (15-25 C.).
- Package 1 is dissolved in 180 ml. of cool tap water (20 C.) and whipped in a Sunbeam Mixmaster at high speed for four minutes to a foam having stiff peaks. Then package 2 is folded into the foam with mild mixing in the mechanical beater. When all of package 2 is added, the mixture is whipped at high speed for one minute.
- the product has a volume of about 4 standard measuring cups, a smooth creamy texture with a firm body and a high gloss. When the icing is spread on a cake, it is found to retain its original texture, body and gloss without syneresis for a period over 72 hours.
- EXAMPLE 4 The gel dried product of the process in Example 1 is substituted in the mix formula in Example 3 for the sol dried carbamino gelatin.
- An icing substantially the same as that produced in Example 3 can be obtained following the same recipe except that package 1 is dissolved in 65 C. water to dissolve the carbamino gelatin, after which the solution is cooled to room temperature and whipped as in Example 3.
- EXAMPLE 5 M arsh mallow gms. of cane syrup and 800 gms. of sucrose are added to 388 ml. of tap water and the mixture is heated to 100 C. 15.4 gms. of carbamino gelatin prepared according to the process in Example 1 from 240 bloom neutral gelatin are added to 100 ml. of tap water heated to 65 C. The two mixtures are combined and cooled to 60 C. and beaten in a Hobart mixer. After 21 minutes of beating, a marshmallow having an overrun of 300% and substantially free of syneresis is produced.
- marshmallow as pigskin gelatin but when modified in accordance with the present invention, it surpasses the performance of all types of unmodified gelatin.
- the method of preparing a gelatin derivative which comprises adjusting a gelatin solution to an alkaline pH by means of calcium'hydroxide, and reacting carbon diclaim 1.
- the method of preparing a gelatin derivative which comprises adjusting a gelatin solution to an alkaline pH by means of calcium hydroxide, reacting carbon dioxide therewith, and drying the resulting solution while maintaining it in the sol state.
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- Chemical & Material Sciences (AREA)
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Description
United States PatenfO GELATIN DERIVATIVES AND THEIR PREPARATION No Drawing. Application January 3,.1956
' Serial No. 556,796
6 Claims. (Cl. 260-117) This invention relates to the production of a gelatin derivative.
It has been found that when a gelatin solution is adjusted to an alkaline pH with calcium hydroxide, and carbon dioxide is reacted with this adjusted solution, a gelatin derivative is formed having improved physical properties. especially suited for whipping. In the process of the invention, sufiicient calcium hydroxide is added to a gelatin solution such as acid or neutral gelatin, to raise its pH to about 9. Neutral gelatin is preferred due to a greater number of carboxyl groups that can react in formation of the derivative. Carbon dioxide is introduced in either gaseous or solid form, the preferred method being to simply bubble carbon dioxide into the reaction mixture.
While it is not definitely determined, it is believed that the derivative produced involves the reaction of carbon dioxide and calcium ions with carboxy and amino groups in the gelatin molecule. For convenience, the gelatin derivative will be referred to as carbamino gelatin.
This gelatin derivative has shown improvements in viscosity and bloom over the unmodified gelatin. As a whipping agent, it produces a larger overrun in a shorter period of Whipping time than unmodified gelatin samples. A stable foam is formed which holds its volume and texture. The carbamino gelatin can be used as a whipping agent in the production of any of the edible or inedible foams in which gelatin, or gelatin plus other whipping adjuncts such as hydrolyzed soy protein are employed. Examples of whipping compositions in which this gelatin derivative can be used successfully are marshmallow preparations, chilfon desserts, icings, and sugar whips generally.
The following are examples of the process of the present invention and the use of the product.
EXAMPLE 1 Calcium hydroxide is dispersed in an aqueous solution of neutral 250 bloom gelatin to raise the pH of the solution to about 9. An excess of carbon dioxide gas is then bubbled into the reaction mixture until the mixture is brought down to about pH 7. As the carbon dioxide is bubbled into the reaction mixture, the gelatin derivative of the present invention is formed and calcium carbonate is precipitated. Excess calcium salts (calcium carbonate and calcium hydroxide) are removed by suitable ion exchange resins. The solution containing the derivative is allowed to gel, and then is tunnel dried and ground. The product is more easily dispersed than the unmodified gelatin starting material and is soluble in water at 65 C.
EXAMPLE 2 Carbamino gelatin, substantially soluble in cold water, is prepared according to the following method: 88.9 lbs. of water are weighed out into a jacketed kettle. 11.1 lbs. of 250 bloom gelatin are added to the cold water with agitation, and the gelatin dispersion is heated to 2,834,771 Patented May 13, 1958 40-45 C. to dissolve the gelatin. Calcium hydroxide is added to the hot gelatin solution until the pH is raised to between 9.5 and 10.0. Carbon dioxide is then bubbled through the gelatin solution for 15 minutes while the pH of the solution is maintained between 9.5 and 10.0 by the addition of calcium hydroxide. The reaction mixture is filtered to remove undissolved lime and calcium carbonate and is placed back into the jacketed kettle with Rohm and Haas IR45 and IR mixed ion exchange resin to remove extraneous anions and cations. After the mixture has been stirred for 15-20 minutes to allow the ion exchange resin to react and a constant pH of about 5 is reached, the solution is filtered again to remove the ion exchange material. Theproduct solution is then dried in the sol state by drying on a double drum drier, although any method of drying the gelatin derivatives whereby the sol state is preserved during dehydration is acceptable. The dried product is ground in a Fitzpatrick mill. The dried prodnot is soluble in relatively cold water (15-25 C.).
EXAMPLE 3 White sugar icing mix PACKAGE. 1
Gms. Sucrose 39.7 Methyl cellulose (Methocel) 1.5 Sol dried carbamino gelatin of Example 2 v 4.0
PACKAGE 2 Sucrose 242.0 Pregelatinized potato starch 10.8 Ethyl vanillin 0.8
Package 1 is dissolved in 180 ml. of cool tap water (20 C.) and whipped in a Sunbeam Mixmaster at high speed for four minutes to a foam having stiff peaks. Then package 2 is folded into the foam with mild mixing in the mechanical beater. When all of package 2 is added, the mixture is whipped at high speed for one minute. The product has a volume of about 4 standard measuring cups, a smooth creamy texture with a firm body and a high gloss. When the icing is spread on a cake, it is found to retain its original texture, body and gloss without syneresis for a period over 72 hours.
EXAMPLE 4 The gel dried product of the process in Example 1 is substituted in the mix formula in Example 3 for the sol dried carbamino gelatin. An icing substantially the same as that produced in Example 3 can be obtained following the same recipe except that package 1 is dissolved in 65 C. water to dissolve the carbamino gelatin, after which the solution is cooled to room temperature and whipped as in Example 3.
EXAMPLE 5 M arsh mallow gms. of cane syrup and 800 gms. of sucrose are added to 388 ml. of tap water and the mixture is heated to 100 C. 15.4 gms. of carbamino gelatin prepared according to the process in Example 1 from 240 bloom neutral gelatin are added to 100 ml. of tap water heated to 65 C. The two mixtures are combined and cooled to 60 C. and beaten in a Hobart mixer. After 21 minutes of beating, a marshmallow having an overrun of 300% and substantially free of syneresis is produced. This is a signifiicant improvement over the overrun produced by employing unmodified gelatin in marshmallow, the best of which is pigskin gelatin providing an overrun of 288% under comparable conditions. Normally neutral gelatin does not possess as high an overrun in 9 by means of calcium hydroxide, and
marshmallow as pigskin gelatin but when modified in accordance with the present invention, it surpasses the performance of all types of unmodified gelatin.
It will be understood that while the invention has been described in part by means of specific examples reference should be had to the appended claims for a definition of the scope of the invention.
What is claimed is:
l. The method of preparing a gelatin derivative which comprises adjusting a gelatin solution to an alkaline pH by means of calcium'hydroxide, and reacting carbon diclaim 1.
3. The method of preparing a gelatin derivative which comprises adjusting a gelatin solution to a pH of about reacting carbon dioxide therewith.
4. The method of preparing a gelatin derivative which comprises adjusting a gelatin solution to a pH of about 9 by means of calcium hydroxide, and reacting carbon dioxide gas therewith.
5. The method of preparing a gelatin derivative which comprises adjusting a gelatin solution to an alkaline pH by means of calcium hydroxide, reacting carbon dioxide therewith, and drying the resulting solution while maintaining it in the sol state.
6. The method of preparing a gelatin derivative which comprises adjusting a gelatin solution to an alkaline pH, by means of calcium hydroxide, and reacting an excess of carbon dioxide therewith. 1
References Cited in the file of this patent UNITED STATES PATENTS 1,993,289 Stokes et al Mar. 5, 1935 2,158,117 Grettie May 16, 1939 2,392,291 Strenitz Jan. 1, 1946
Claims (2)
1. THE METHOD OF PREPARING A GELATIN DERIVATIVE WHICH COMPRISES ADJUSTING A GELATIN SOLUTION TO AN ALKALINE PH BY MEANS OF CALCIUM HYDROXIDE, AND REACTING CARBON DIOXIDE THEREWITH.
5. THE METHOD OF PREPARING A GELATIN DERIVATIVE WHICH COMPRISES ADJUSTING A GELATIN SOLUTION TO AN ALKALINE PH BY MEANS OF CALCIUM HYDROXIDE, REACTING CARBON DIOXIDE THEREWITH, AND DRYING THE RESULTING SOLUTION WHILE MAINTAINING IT IN THE SOL STATE.
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Application Number | Priority Date | Filing Date | Title |
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US556796A US2834771A (en) | 1956-01-03 | 1956-01-03 | Gelatin derivatives and their preparation |
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Application Number | Priority Date | Filing Date | Title |
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US556796A US2834771A (en) | 1956-01-03 | 1956-01-03 | Gelatin derivatives and their preparation |
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US2834771A true US2834771A (en) | 1958-05-13 |
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US556796A Expired - Lifetime US2834771A (en) | 1956-01-03 | 1956-01-03 | Gelatin derivatives and their preparation |
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2992213A (en) * | 1957-11-08 | 1961-07-11 | Eastman Kodak Co | Acid cooked pigskin gelatins for photographic subbing |
US3475404A (en) * | 1966-08-25 | 1969-10-28 | Wilson Pharm & Chem Corp | Method of preparing proteinaceous material which comprises heating an aqueous solution of collagencontaining material at a temperature in the range of 250 f.-350 f. and then treating the solution with anion exchange resins |
US3683939A (en) * | 1970-05-28 | 1972-08-15 | Wilson Pharm & Chem Corp | Proteinaceous cosmetic material for hair conditioning |
US3765917A (en) * | 1970-11-24 | 1973-10-16 | Ken Hayashibara O | Shaped body of gelatin containing amylose and/or amylitol |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1993289A (en) * | 1933-02-18 | 1935-03-05 | Royal Baking Powder Co | Gelatin food product and method of preparing same |
US2158117A (en) * | 1938-08-23 | 1939-05-16 | Ind Patents Corp | Gelatin treatment |
US2392297A (en) * | 1942-03-06 | 1946-01-01 | Ind Patents Corp | Method of making finely divided gelatin products |
-
1956
- 1956-01-03 US US556796A patent/US2834771A/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1993289A (en) * | 1933-02-18 | 1935-03-05 | Royal Baking Powder Co | Gelatin food product and method of preparing same |
US2158117A (en) * | 1938-08-23 | 1939-05-16 | Ind Patents Corp | Gelatin treatment |
US2392297A (en) * | 1942-03-06 | 1946-01-01 | Ind Patents Corp | Method of making finely divided gelatin products |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2992213A (en) * | 1957-11-08 | 1961-07-11 | Eastman Kodak Co | Acid cooked pigskin gelatins for photographic subbing |
US3475404A (en) * | 1966-08-25 | 1969-10-28 | Wilson Pharm & Chem Corp | Method of preparing proteinaceous material which comprises heating an aqueous solution of collagencontaining material at a temperature in the range of 250 f.-350 f. and then treating the solution with anion exchange resins |
US3683939A (en) * | 1970-05-28 | 1972-08-15 | Wilson Pharm & Chem Corp | Proteinaceous cosmetic material for hair conditioning |
US3765917A (en) * | 1970-11-24 | 1973-10-16 | Ken Hayashibara O | Shaped body of gelatin containing amylose and/or amylitol |
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